A condition caused by a deficiency of PARATHYROID HORMONE (or PTH). It is characterized by HYPOCALCEMIA and hyperphosphatemia. Hypocalcemia leads to TETANY. The acquired form is due to removal or injuries to the PARATHYROID GLANDS. The congenital form is due to mutations of genes, such as TBX1; (see DIGEORGE SYNDROME); CASR encoding CALCIUM-SENSING RECEPTOR; or PTH encoding parathyroid hormone
1
Hypopharyngeal Neoplasms -- therapy : Treatment of esophageal and hypopharyngeal squamous cell carcinoma / Giovanni de Manzoni (ed.) ; in collaboration with Simone Giacopuzzi, Andrea Zanoni ; forewords by Gianluigi Melotti, Claudio Cordiano
Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures
Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures
A small, unpaired gland situated in the SELLA TURCICA. It is connected to the HYPOTHALAMUS by a short stalk which is called the INFUNDIBULUM --consider also terms at HYPOPHYS-
A small, unpaired gland situated in the SELLA TURCICA. It is connected to the HYPOTHALAMUS by a short stalk which is called the INFUNDIBULUM --consider also terms at HYPOPHYS-
A small, unpaired gland situated in the SELLA TURCICA. It is connected to the HYPOTHALAMUS by a short stalk which is called the INFUNDIBULUM --consider also terms at HYPOPHYS-
1
Hypophysectomie. : Pituitary surgery : a modern approach / volume editors, Edward R. Laws, Jr., Jason P. Sheehan
2006
1
Hypophysen-Zwischenhirn-System : Hypothalamic-pituitary development : genetic and clinical aspects / volume editors, Raphaël Rappaport, Serge Amselem
A small, unpaired gland situated in the SELLA TURCICA. It is connected to the HYPOTHALAMUS by a short stalk which is called the INFUNDIBULUM --consider also terms at HYPOPHYS-
A small, unpaired gland situated in the SELLA TURCICA. It is connected to the HYPOTHALAMUS by a short stalk which is called the INFUNDIBULUM --consider also terms at HYPOPHYS-
A small, unpaired gland situated in the SELLA TURCICA. It is connected to the HYPOTHALAMUS by a short stalk which is called the INFUNDIBULUM --consider also terms at HYPOPHYS-
1
Hypopituitarism -- complications : Growth hormone deficiency in adults / volume editors, Jens Otto Lunde Jorgensen, Jens Sandahl Christiansen
2005
1
Hypopituitarism -- etiology : Growth hormone deficiency in adults / volume editors, Jens Otto Lunde Jorgensen, Jens Sandahl Christiansen
2005
1
Hypopituitarism -- therapy : Growth hormone deficiency in adults / volume editors, Jens Otto Lunde Jorgensen, Jens Sandahl Christiansen
Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cell immunodeficiency, HYPOCALCEMIA, defects in the outflow tract of the heart, and craniofacial anomalies
Disorders characterized by multiple cessations of respirations during sleep that induce partial arousals and interfere with the maintenance of sleep. Sleep apnea syndromes are divided into central (see SLEEP APNEA, CENTRAL), obstructive (see SLEEP APNEA, OBSTRUCTIVE), and mixed central-obstructive types
Disorders characterized by multiple cessations of respirations during sleep that induce partial arousals and interfere with the maintenance of sleep. Sleep apnea syndromes are divided into central (see SLEEP APNEA, CENTRAL), obstructive (see SLEEP APNEA, OBSTRUCTIVE), and mixed central-obstructive types
An abnormal response to a stimulus applied to the sensory components of the nervous system. This may take the form of increased, decreased, or absent reflexes
